ALBERT HEISS Forceps - Indonesia BPOM Medical Device Registration
ALBERT HEISS Forceps is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203220127. The device is manufactured by ALBERT HEISS GMBH & CO. KG. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SURYA TAMA MEDIKA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 1
Manufacturer
ALBERT HEISS GMBH & CO. KG.Country of Origin
Germany
Authorized Representative
PT. SURYA TAMA MEDIKAAR Address
Jl m hasibuan ruko suncity pbb. 37 real blok e.27 rt 004 rw 002 kel margajaya kec bekasi selatan kota bekasi
Registration Date
Jan 01, 2023
Expiry Date
Jan 01, 2027
Product Type
Surgical Eye Equipment
Manual ophthalmic surgical instrument.
Non Electromedic Sterile
ALBERT HEISS Titanium Instruments
ALBERT HEISS Needle Holders
ALBERT HEISS Speculums
ALBERT HEISS Hooks, Spatulas and Manipulators
ALBERT HEISS Sharp Instruments
ALBERT HEISS Probes and Dilators
ALBERT HEISS Marker
ALBERT HEISS Towel Clamp
ALBERT HEISS Cannula
ALBERT HEISS Hammer
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